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Hi all,
Taking a picture of the cross-section of a nerve at 200x shows the entire nerve, but the axons/fibers are too small to be seen/counted. So what I would like to do is take 4 separate pictures of the 4 quadrants of the nerve at 400x, and then be able to combine them into a single image. Is there a way in imageJ to automatically account for the overlap of the 4 images? Thank you |
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Hi, Does this look helpful? http://bigwww.epfl.ch/thevenaz/mosaicj/ I plan to try this myself soon, but haven't yet used it. I'd be glad to hear how you get on. Best, Ed |
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2011/10/7 edsimmons <[hidden email]>:
> GloryField wrote: >> >> Hi all, >> >> Taking a picture of the cross-section of a nerve at 200x shows the entire >> nerve, but the axons/fibers are too small to be seen/counted. So what I >> would like to do is take 4 separate pictures of the 4 quadrants of the >> nerve at 400x, and then be able to combine them into a single image. Is >> there a way in imageJ to automatically account for the overlap of the 4 >> images? Stitching plugin for images or stacks (translation only): http://fiji.sc/wiki/index.php/Stitching_2D/3D TrakEM2 plugin for montages (from translation only to elastic registration): http://fiji.sc/wiki/index.php/TrakEM2 (see for example: http://fiji.sc/wiki/index.php/File:Trakem2-snap.jpg ) Hope that helps. Albert -- http://albert.rierol.net http://www.ini.uzh.ch/~acardona/ |
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In reply to this post by edsimmons
Hi,
Fiji has stitching plugin that works well to combine overlapping images. Rainer On 10/7/11 9:01 AM, edsimmons wrote: > GloryField wrote: >> Hi all, >> >> Taking a picture of the cross-section of a nerve at 200x shows the entire >> nerve, but the axons/fibers are too small to be seen/counted. So what I >> would like to do is take 4 separate pictures of the 4 quadrants of the >> nerve at 400x, and then be able to combine them into a single image. Is >> there a way in imageJ to automatically account for the overlap of the 4 >> images? >> >> Thank you >> > Hi, > > Does this look helpful? > > http://bigwww.epfl.ch/thevenaz/mosaicj/ > > I plan to try this myself soon, but haven't yet used it. I'd be glad to hear > how you get on. > > Best, > Ed > > -- > View this message in context: http://imagej.588099.n2.nabble.com/Combining-image-panoramic-tp6867276p6869227.html > Sent from the ImageJ mailing list archive at Nabble.com. ... [show rest of quote] -- Rainer Kohler, Ph.D Assistant in Research Office Phone: 617 643 6391 Cell Phone: 978 578 5057 E.mail: [hidden email] Center for Systems Biology Massachusetts General Hospital Richard B. Simches Research Center 185 Cambridge Street Suite 5.210 Boston, MA 02114 Phone: (617) 643-0500 The information in this e-mail is intended only for the person to whom it is addressed. If you believe this e-mail was sent to you in error and the e-mail contains patient information, please contact the Partners Compliance HelpLine at http://www.partners.org/complianceline . If the e-mail was sent to you in error but does not contain patient information, please contact the sender and properly dispose of the e-mail. |
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thank you all, I tried the stitching directory with unknown configuration in FIJI and it worked great!
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Another question about using the analyze particles in ImageJ/FIJI
here's a sample image I made using stitching: http://www.swapdrive.com/file.asp?ID=tG+4c+dQUV2uaBUzGE9QXIqvYD6NpPr0zU3HMp4maEzHuo55/04pqQ==url I'm trying to measure the average area of each of the axons within the nerve, including the myelin sheath. What I did so far is: Process>Subtract Background>5 pixels Process>Binary>Make Binary Analyze>Analyze Particles>Size 4-350, circularity 0.25-1.0, show outlines, include holes I chose 350 as max size because that allows me to eliminate blood vessels within the nerve. I arbitrarily chose 0.25 circularity because I didn't know what else to pick. Doing this gave me an average size of 50.668 pixels. I will put a slide with a length marker under microscope with same magnification so I can use "Analyze > Set Scale" and get values in micrometers. Do you guys think this would be an OK way of measuring the axon cross section area? Thank you again! |
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